Allele Registry

Canonical Allele Identifier: PA2826465041

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000501150

RCV003449402

ClinVar Variation:

433893

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser610Leu	CA346729109 NM_001258281.1:c.1829C>T